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Recruiting NCT06973642

NCT06973642 Evaluation of Home-based Telerehabilitation Platform to Augment Orthopedic Rehabilitation

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Clinical Trial Summary
NCT ID NCT06973642
Status Recruiting
Phase
Sponsor University of Mississippi Medical Center
Condition Anterior Cruciate Ligament Reconstruction Rehabilitation
Study Type INTERVENTIONAL
Enrollment 15 participants
Start Date 2025-06-01
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Software as a Medical Device (WizeCare)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 15 participants in total. It began in 2025-06-01 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this study is to assess the feasibility of utilizing a telehealth rehabilitation platform to increase patient access for individuals who have undergone orthopedic surgery. Patient participants will be seen via telehealth until they are able to be seen by an in-person physical therapist of their choice. Provider participants will be the physical therapist who are providing physical therapy services through the telehealth application. Data collection: Patient and provider post surveys Home program and scheduled visit compliance rate Healthcare information in keeping with Stand of care physical therapy practices Feasibility criteria will be assessed to determine whether this modality improves physical therapy access for patients living in rural areas.

Eligibility Criteria

Inclusion Criteria: * Patients that are candidates for anterior cruciate ligament reconstruction. Exclusion Criteria: * Visual impairment greater than 20/200 with the use of corrective lenses * Does not own or have consistent access to a phone with data capabilities * Has been informed by their healthcare provider that they should not participate in physical therapy services * Participants can be excluded from the study at any time if the physical therapist determines the patient is not an appropriate candidate for telehealth therapy.

Contact & Investigator

Central Contact

Jacob Daniels, DPT, EdD

✉ jbdaniels@umc.edu

📞 6018154038

Frequently Asked Questions

Who can join the NCT06973642 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Anterior Cruciate Ligament Reconstruction Rehabilitation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06973642 currently recruiting?

Yes, NCT06973642 is actively recruiting participants. Contact the research team at jbdaniels@umc.edu for enrollment information.

Where is the NCT06973642 trial being conducted?

This trial is being conducted at Jackson, United States.

Who is sponsoring the NCT06973642 clinical trial?

NCT06973642 is sponsored by University of Mississippi Medical Center. The trial plans to enroll 15 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology